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Abdussalam Azem

Showing results (61-70 of 74) with videos related to

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Plos One|December 11, 2012
Identification of elements that dictate the specificity of mitochondrial Hsp60 for its co-chaperoninAvital Parnas, Shahar Nisemblat, Celeste Weiss, et al.
The Journal of Biological Chemistry|October 8, 2013
Crystal and solution studies of the "Plus-C" odorant-binding protein 48 from Anopheles gambiae: control of binding specificity through three-dimensional domain swappingKaterina E Tsitsanou, Christina E Drakou, Trias Thireou, et al.
Science Advances|March 4, 2026
Structural remodeling of the mitochondrial protein biogenesis machinery under proteostatic stressKenneth Ehses, Jorge P López-Alonso, Odetta Antico, et al.
Nature Communications|April 23, 2020
Structural basis for active single and double ring complexes in human mitochondrial Hsp60-Hsp10 chaperoninYacob Gomez-Llorente, Fady Jebara, Malay Patra, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian AuthorityAnja K Mayer, Ghassan Balousha, Rajech Sharkia, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Structural basis for ATP-driven double-ring assembly of the human mitochondrial Hsp60 chaperoninIgor Tascón, Jorge P López-Alonso, Yoel Shkolnisky, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathyRajech Sharkia, Stavit A Shalev, Abdelnaser Zalan, et al.
Frontiers in Molecular Biosciences|October 25, 2016
Effects of a Mutation in the <i>HSPE1</i> Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental DisorderAnne S Bie, Paula Fernandez-Guerra, Rune I D Birkler, et al.
European Journal of Human Genetics : EJHG|March 28, 2020
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discoveryHolger Hengel, Rebecca Buchert, Marc Sturm, et al.
European Journal of Human Genetics : EJHG|May 29, 2021
Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discoveryHolger Hengel, Rebecca Buchert, Marc Sturm, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Plos One|December 11, 2012
Identification of elements that dictate the specificity of mitochondrial Hsp60 for its co-chaperoninAvital Parnas, Shahar Nisemblat, Celeste Weiss, et al.
The Journal of Biological Chemistry|October 8, 2013
Crystal and solution studies of the "Plus-C" odorant-binding protein 48 from Anopheles gambiae: control of binding specificity through three-dimensional domain swappingKaterina E Tsitsanou, Christina E Drakou, Trias Thireou, et al.
Science Advances|March 4, 2026
Structural remodeling of the mitochondrial protein biogenesis machinery under proteostatic stressKenneth Ehses, Jorge P López-Alonso, Odetta Antico, et al.
Nature Communications|April 23, 2020
Structural basis for active single and double ring complexes in human mitochondrial Hsp60-Hsp10 chaperoninYacob Gomez-Llorente, Fady Jebara, Malay Patra, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian AuthorityAnja K Mayer, Ghassan Balousha, Rajech Sharkia, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Structural basis for ATP-driven double-ring assembly of the human mitochondrial Hsp60 chaperoninIgor Tascón, Jorge P López-Alonso, Yoel Shkolnisky, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathyRajech Sharkia, Stavit A Shalev, Abdelnaser Zalan, et al.
Frontiers in Molecular Biosciences|October 25, 2016
Effects of a Mutation in the <i>HSPE1</i> Gene Encoding the Mitochondrial Co-chaperonin HSP10 and Its Potential Association with a Neurological and Developmental DisorderAnne S Bie, Paula Fernandez-Guerra, Rune I D Birkler, et al.
European Journal of Human Genetics : EJHG|March 28, 2020
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discoveryHolger Hengel, Rebecca Buchert, Marc Sturm, et al.
European Journal of Human Genetics : EJHG|May 29, 2021
Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discoveryHolger Hengel, Rebecca Buchert, Marc Sturm, et al.
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